A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11240



Internal ID15539339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69516587..69533149hg38UCSC Ensembl
Outerchr10:71276343..71292905hg19UCSC Ensembl
Outerchr10:70946349..70962911hg18UCSC Ensembl
Outerchr10:70946349..70962911hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3816563
hg1916563
hg1816563
hg1716563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7021
Supporting Variants
SamplesNA15510
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv11240
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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